Canonical Allele Identifier: CA884820038

Gene: AGRN

Linked Data

• dbSNP Id: rs1198227488
• gnomAD v3: 1-1043788-GC-G
• gnomAD v4: 1-1043788-GC-G
• MyVariant Identifiers: chr1:g.979169del (hg19) ; chr1:g.1043789del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1043790del , CM000663.2:g.1043790del	GRCh38
NC_000001.10:g.979170del , CM000663.1:g.979170del	GRCh37
NC_000001.9:g.969033del	NCBI36
NG_016346.1:g.28668del , LRG_198:g.28668del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.1799-33del MANE Select	ENSP00000368678.2:n.1799-33del
ENST00000651234.1:c.1484-33del	ENSP00000499046.1:n.1484-33del
ENST00000652369.1:c.1484-33del	ENSP00000498543.1:n.1484-33del
ENST00000379370.6:c.1799-33del	ENSP00000368678.2:n.1799-33del
ENST00000620552.4:c.1385-33del	ENSP00000484607.1:n.1385-33del
NM_001305275.1:c.1799-33del	NP_001292204.1:n.1799-33del
NM_198576.3:c.1799-33del	NP_940978.2:n.1799-33del
XM_005244749.2:c.1799-33del	XP_005244806.1:n.1799-33del
XM_006710635.2:c.1799-33del	XP_006710698.1:n.1799-33del
XM_011541429.1:c.1799-33del	XP_011539731.1:n.1799-33del
XM_011541430.1:c.926-33del	XP_011539732.1:n.926-33del
XM_011541431.1:c.65-33del	XP_011539733.1:n.65-33del
XR_946650.1:n.1866-33del
NM_001364727.1:c.1484-33del	NP_001351656.1:n.1484-33del
XM_005244749.3:c.1799-33del	XP_005244806.1:n.1799-33del
XM_011541429.2:c.1799-33del	XP_011539731.1:n.1799-33del
XR_946650.2:n.1870-33del
NM_001305275.2:c.1799-33del	NP_001292204.1:n.1799-33del
NM_198576.4:c.1799-33del MANE Select	NP_940978.2:n.1799-33del
NM_001364727.2:c.1484-33del	NP_001351656.1:n.1484-33del